Camorani Simona, Fedele Monica, Zannetti Antonella, Cerchia Laura
Istituto per l'Endocrinologia e l'Oncologia Sperimentale G. Salvatore (IEOS), CNR, 80145 Naples, Italy.
Istituto di Biostrutture e Bioimmagini, CNR, 80145 Naples, Italy.
Pharmaceuticals (Basel). 2018 Nov 13;11(4):123. doi: 10.3390/ph11040123.
Compared to other breast cancers, triple-negative breast cancer (TNBC) usually affects younger patients, is larger in size, of higher grade and is biologically more aggressive. To date, conventional cytotoxic chemotherapy remains the only available treatment for TNBC because it lacks expression of the estrogen receptor (ER), progesterone receptor (PR) and epidermal growth factor receptor 2 (HER2), and no alternative targetable molecules have been identified so far. The high biological and clinical heterogeneity adds a further challenge to TNBC management and requires the identification of new biomarkers to improve detection by imaging, thus allowing the specific treatment of each individual TNBC subtype. The Systematic Evolution of Ligands by EXponential enrichment (SELEX) technique holds great promise to the search for novel targetable biomarkers, and aptamer-based molecular approaches have the potential to overcome obstacles of current imaging and therapy modalities. In this review, we highlight recent advances in oligonucleotide aptamers used as imaging and/or therapeutic agents in TNBC, discussing the potential options to discover, image and hit new actionable targets in TNBC.
与其他乳腺癌相比,三阴性乳腺癌(TNBC)通常影响较年轻的患者,肿瘤体积更大,分级更高,生物学行为更具侵袭性。迄今为止,传统的细胞毒性化疗仍然是TNBC唯一可用的治疗方法,因为它缺乏雌激素受体(ER)、孕激素受体(PR)和表皮生长因子受体2(HER2)的表达,并且目前尚未发现其他可靶向的分子。高度的生物学和临床异质性给TNBC的治疗带来了进一步的挑战,需要识别新的生物标志物以改善影像学检测,从而实现对每个TNBC亚型的个体化治疗。指数富集的配体系统进化(SELEX)技术在寻找新型可靶向生物标志物方面具有巨大潜力,基于适配体的分子方法有可能克服当前成像和治疗方式的障碍。在本综述中,我们重点介绍了寡核苷酸适配体在TNBC中用作成像和/或治疗剂的最新进展,讨论了发现、成像和靶向TNBC新的可操作靶点的潜在选择。